Quality Assurance Specialist

3 days ago


Louisville, Kentucky, United States ZeoChem Full time
Job Title: Quality Systems Coordinator

Zeochem is seeking a highly skilled Quality Systems Coordinator to oversee the quality assurance program for its chemical manufacturing facility in Louisville, KY.

Key Responsibilities:
  • Maintain and implement quality processes and procedures for site quality systems
  • Lead local Quality Improvement Team (QIT) meetings and implement the local Continuous Improvement Process program
  • Draft quality assurance policies and procedures, interpret and implement quality assurance standards and procedures, and evaluate the adequacy of quality assurance standards
  • Document internal audits and other quality assurance activities, investigate customer complaints and non-conformance issues, and ensure customer resolution
  • Maintain Safety Data Sheet systems and monitor compliance to all applicable regulations for adsorbent product lines
  • Analyze data to identify areas for improvement in the quality system, develop and recommend corrective and preventive actions, and prepare reports to communicate outcomes of quality activities
  • Identify training needs and organize training interventions to meet quality standards, coordinate and support on-site audits conducted by external providers, and evaluate audit findings and implement appropriate corrective actions
  • Monitor risk management activities, responsible for document management systems, including contracts, and assure ongoing compliance with quality and industry regulatory requirements
Requirements:
  • Bachelor's degree preferred
  • 5+ years' experience in Quality Assurance
  • Certified ISO auditor preferred
  • Certifications including Quality Auditor, Quality Engineer, Quality Improvement Associate, or Six Sigma preferred
  • Quality inspection, auditing, and testing experience
  • Strong computer skills including Microsoft Office, QA applications and databases
  • Proven experience managing projects and ability to meet deadlines
  • Strong written, communications, and interpersonal relationship skills
  • Ability to present data and presentations across multiple levels
  • Strong Organization Skills
  • Experience with implementation of corrective action programs
  • Molecular Sieve or industry-related experience desired
  • Knowledge of tools, concepts, and methodologies of QA
  • Knowledge of relevant regulatory requirements
Work Environment:

The work environment is quiet, and the employee is occasionally exposed to moving mechanical parts, fumes or airborne particles, and toxic or caustic chemicals.

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.



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